NCOA7 - nuclear receptor coactivator 7 Gene

Also Known as ESNA1; TLDC4; ERAP140; NCOA7-AS; Nbla00052; Nbla10993; dJ187J11.3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 135112

About NCOA7

Cytogenetic location: 6q22.31-q22.32 Genomic coordinates (GRCh38): 6:125,781,115-125,932,034 (from NCBI)

This gene has 11 transcripts (splice variants), 295 orthologues and 3 paralogues. Ubiquitous expression in urinary bladder (RPKM 17.8), adrenal (RPKM 16.0) and 25 other tissues.

Summary

Enables nuclear receptor binding activity and nuclear receptor coactivator activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

NCOA7 Products (6)

mRNA Protein Name
NM_001122842.3 NP_001116314.1 nuclear receptor coactivator 7 isoform 2
NM_001199619.2 NP_001186548.1 nuclear receptor coactivator 7 isoform 1
NM_001199620.2 NP_001186549.1 nuclear receptor coactivator 7 isoform 1
NM_001199621.2 NP_001186550.1 nuclear receptor coactivator 7 isoform 3
NM_001199622.2 NP_001186551.1 nuclear receptor coactivator 7 isoform 4
NM_181782.5 NP_861447.3 nuclear receptor coactivator 7 isoform 1
Molecular Function GO Annotation Evidence Verweise Source
enables nuclear receptor binding IDA
IDA: Inferred from direct assay
11971969 GOA
enables nuclear receptor coactivator activity IDA
IDA: Inferred from direct assay
11971969 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10395741 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
11971969 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

NCOA7 Protein Structure

LysM

LysM: LysM domain (120 - 158)

TLD

TLD: TLD (806 - 941)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 942 a.a.
Protein Preferred Names Protein Names

nuclear receptor coactivator 7

  • 140 kDa estrogen receptor-associated protein

NCOA7 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
NCOA7 Q8NI08 DIRAS1 Homo sapiens O95057 33961781
Intra
NCOA7 Q8NI08 MAP1LC3C Homo sapiens Q9BXW4 20562859
Intra
NCOA7 Q8NI08 MAP1LC3B Homo sapiens Q9GZQ8 20562859
Intra
NCOA7 Q8NI08 GABARAP Homo sapiens O95166 20562859
Intra
NCOA7 Q8NI08 GABARAPL2 Homo sapiens P60520 20562859
Intra
NCOA7 Q8NI08 GABARAPL1 Homo sapiens Q9H0R8 20562859
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, And Seizures Syndrome
  • Door Syndrome

  • Doors Syndrome

  • Digitorenocerebral Syndrome

  • Autosomal Recessive Deafness-Onychodystrophy Syndrome

  • Deafness-Onychoosteodystrophy-Intellectual Disability Syndrome

  • DOORS

  • Drc Syndrome

  • Eronen Syndrome

  • Deafness-Onychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

  • Brachydactyly Due To Absence Of Distal Phalanges

  • Deafness-Onychodystrophy-Osteodystrophy-Intellectual Disability-Seizures Syndrome

  • Deafness, Onychodystrophy, Osteodystrophy, And Mental Retardation Syndrome

  • Deafness-Oncychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

  • Autosomal Recessive Hearing Loss-Onychodystrophy Syndrome

  • Hearing Loss-Onychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

  • Hearing Loss-Onychodystrophy-Osteodystrophy-Intellectual Disability-Seizures Syndrome

  • Hearing Loss-Onychoosteodystrophy-Intellectual Disability Syndrome

  • Deafness, Onychodystrophy, Osteodystrophy, Intellectual Disability, And Seizures Syndrome

  • Deafness, Congenital Onychodystrophy, Recessive Form

  • Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation Syndrome

Developmental And Epileptic Encephalopathy 16
  • DEE16

  • Epileptic Encephalopathy, Early Infantile, 16

  • Eiee16

  • Developmental And Epileptic Encephalopathy, 16

  • Early Infantile Epileptic Encephalopathy 16

  • Progressive Myoclonic Epilepsy With Dystonia

  • Pmed

  • Progressive Myoclonus Epilepsy With Dystonia

  • Encephalopathy, Epileptic, Early Infantile, Type 16

Brugada Syndrome
  • Sudden Unexpected Nocturnal Death Syndrome

  • Sudden Unexplained Nocturnal Death Syndrome

  • Bangungut

  • Brugada Type Idiopathic Ventricular Fibrillation

  • Pokkuri Death Syndrome

  • Sunds

  • Idiopathic Ventricular Fibrillation, Brugada Type

  • Sudden Unexplained Death

  • Dream Disease

  • Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome

  • Sudden Unexplained Death Syndrome

  • Suds

  • Sunds - [Sudden Unexplained Nocturnal Death Syndrome]

Martsolf Syndrome 1
  • Martsolf Syndrome

  • Cataract-Intellectual Disability-Hypogonadism Syndrome

  • MARTS1

  • Marts

  • Cataract-Mental Retardation-Hypogonadism

  • Martsolf

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus NCOA7 RGD RGD:1566426
Felis catus NCOA7 VGNC VGNC:63743
Macaca mulatta NCOA7 VGNC VGNC:74998
Mus musculus NCOA7 MGD MGI:2444847
Canis familiaris NCOA7 VGNC VGNC:43664
Bos taurus NCOA7 VGNC VGNC:108132
Others NCOA7 NCBI